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1
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33646803175
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For recent publications concerning the synthesis and biological activity of 1,2,3-triazoles, see:
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3
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0038025786
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Tullis J.S., VanRens J.C., Natchus M.G., Clark M.P., Janusz B., De M.J., and Janusz L.C.H. Bioorg. Med. Chem. Lett. 13 (2003) 1665-1668
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(2003)
Bioorg. Med. Chem. Lett.
, vol.13
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Tullis, J.S.1
VanRens, J.C.2
Natchus, M.G.3
Clark, M.P.4
Janusz, B.5
De, M.J.6
Janusz, L.C.H.7
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5
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26844512576
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Holla B.B.S., Mahalinga M., Karthikeyan M.S., Poojary B., Akberali P.M., and Kumari N.S. Eur. J. Med. Chem. 40 (2005) 1173-1178
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(2005)
Eur. J. Med. Chem.
, vol.40
, pp. 1173-1178
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Holla, B.B.S.1
Mahalinga, M.2
Karthikeyan, M.S.3
Poojary, B.4
Akberali, P.M.5
Kumari, N.S.6
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9
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0037281877
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and references cited therein
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Peng W., and Zhu S. Synlett (2003) 187-190 and references cited therein
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(2003)
Synlett
, pp. 187-190
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Peng, W.1
Zhu, S.2
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10
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0037099395
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Rostovtsev V.V., Green L.G., Fokin V.V., and Sharpless K.B. Angew Chem., Int. Ed. 41 (2002) 2596-2599
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(2002)
Angew Chem., Int. Ed.
, vol.41
, pp. 2596-2599
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Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
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11
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0037454346
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Wang Q., Chan T.R., Fokin V.V., Sharpless K.B., and Finn M. J. Am. Chem. Soc. 125 (2003) 3192-3193
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(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3192-3193
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Wang, Q.1
Chan, T.R.2
Fokin, V.V.3
Sharpless, K.B.4
Finn, M.5
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12
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0042125393
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Lee L.V., Mitchell M.L., Huang S.-J., Fokin V.V., Sharpless K.B., and Wong C.-H. J. Am. Chem. Soc. 125 (2003) 9588-9589
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(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 9588-9589
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Lee, L.V.1
Mitchell, M.L.2
Huang, S.-J.3
Fokin, V.V.4
Sharpless, K.B.5
Wong, C.-H.6
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13
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11844255741
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Himo F., Lovell T., Hilgraf R., Rostovtev V.V., Noodleman L., Sharpless K.B., and Fokin V.V. J. Am. Chem. Soc. 127 (2005) 210-216
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(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 210-216
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Himo, F.1
Lovell, T.2
Hilgraf, R.3
Rostovtev, V.V.4
Noodleman, L.5
Sharpless, K.B.6
Fokin, V.V.7
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24
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33646805254
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For a recent review of the Glaser reaction, see:
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26
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33646794862
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For a recent application of the Glaser coupling, see:
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28
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33947476790
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For Hay's condition, see:
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For Hay's condition, see:. Hay A.S. J. Org. Chem. 27 (1962) 3320-3321
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(1962)
J. Org. Chem.
, vol.27
, pp. 3320-3321
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Hay, A.S.1
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29
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0037127074
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For a recent application of Hay's conditions, see:
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For a recent application of Hay's conditions, see:. Gibtner T., Hampel F., Gisselbretch J.-P., and Hirsch A. Chem.-Eur. J. 68 (2002) 408-432
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(2002)
Chem.-Eur. J.
, vol.68
, pp. 408-432
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Gibtner, T.1
Hampel, F.2
Gisselbretch, J.-P.3
Hirsch, A.4
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31
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33646788286
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note
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Thermal dipolar cycloaddition of 1,6-dimethoxyhexa-2,4-diyne and hydroxy azide 1a (toluene, 8 h, 80 °C) afforded a 3:1 mixture of regioisomeric monotriazoles (isolated yield of 3=59% and regioisomer=21%).
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32
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0034730992
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For 7-endo-dig cyclization of alkynols, see:
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For 7-endo-dig cyclization of alkynols, see:. Trost B.M., and Frontier A.J. J. Am. Chem. Soc. 122 (2000) 11727-11728
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(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11727-11728
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Trost, B.M.1
Frontier, A.J.2
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33
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0035963683
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For a recent report citing the importance of oxygen diffusion in Cu(II)-mediated amination of boronic acids, see:
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For a recent report citing the importance of oxygen diffusion in Cu(II)-mediated amination of boronic acids, see:. Buchwald S.L., and Antilla J.C. Org. Lett. 3 (2001) 2077-2079
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(2001)
Org. Lett.
, vol.3
, pp. 2077-2079
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Buchwald, S.L.1
Antilla, J.C.2
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34
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0035858723
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For use of amine oxides in Cu(II)-catalyzed coupling, see:
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For use of amine oxides in Cu(II)-catalyzed coupling, see:. Lam P.Y.S., Vincent G., Clark C.G., Deudon S., and Jadhav P.K. Tetrahedron Lett. 42 (2001) 3415-3418
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(2001)
Tetrahedron Lett.
, vol.42
, pp. 3415-3418
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Lam, P.Y.S.1
Vincent, G.2
Clark, C.G.3
Deudon, S.4
Jadhav, P.K.5
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35
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33646817630
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2 atmosphere results in the formation of copper(III) species, see:
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36
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37049071250
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Capdevielle P., Sparfel D., Baranne-Lafont J., Kim Cuong N., and Maumy M. J. Chem. Soc., Chem. Commun. (1990) 565-566
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(1990)
J. Chem. Soc., Chem. Commun.
, pp. 565-566
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Capdevielle, P.1
Sparfel, D.2
Baranne-Lafont, J.3
Kim Cuong, N.4
Maumy, M.5
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38
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33646798294
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For examples of a hydroxyl serving as a ligand in Cu(II) amino alcohol complexes, see:
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39
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0035840231
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Choi K.-Y., Lee H.-H., Suh I.H., Kim J.G., and Shin U.-S. Inorg. Chim. Acta 321 (2001) 221-227
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(2001)
Inorg. Chim. Acta
, vol.321
, pp. 221-227
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Choi, K.-Y.1
Lee, H.-H.2
Suh, I.H.3
Kim, J.G.4
Shin, U.-S.5
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41
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17644414186
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For a recent mechanistic study of the Cu(I)-catalyzed azide-alkyne cycloaddition reaction, see:
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For a recent mechanistic study of the Cu(I)-catalyzed azide-alkyne cycloaddition reaction, see:. Rodionov V.O., Fokin V.V., and Finn M.G. Angew. Chem., Int. Ed. 44 (2005) 2210-2215
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(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 2210-2215
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Rodionov, V.O.1
Fokin, V.V.2
Finn, M.G.3
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42
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33646800038
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For a discussion of the role of Cu(III) in reductive-elimination, see:
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44
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33646772040
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For a recent example, see:
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46
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33646814244
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For recent reviews of dicopper-dioxo complexes, see:
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49
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33646801090
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For theoretical calculations proposing dicopper-dioxo complexes in the Glaser coupling, see:
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51
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27644438654
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For recent studies toward the synthesis of 1,4,5-trisubstituted-1,2,3-triazoles, see:
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For recent studies toward the synthesis of 1,4,5-trisubstituted-1,2,3-triazoles, see:. Deng J., Wu Y.-M., and Chen Q.-Y. Synthesis 6 (2005) 2730-2738
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(2005)
Synthesis
, vol.6
, pp. 2730-2738
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Deng, J.1
Wu, Y.-M.2
Chen, Q.-Y.3
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